Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,374 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,374 in last 12 months

Showing 2176121780 of 46,762 recalls

Medical DeviceMarch 18, 2019· Ideal Implant Incorporated

Recalled Item: IDEAL IMPLANT Structured Breast Implant Recalled by Ideal Implant...

The Issue: The implants were deflating due to a piece of silicone disrupting the seal...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to Continuous...

The Issue: Continuous operation at very high tube output may result in increased wear...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2019· Roche Diagnostics Corporation

Recalled Item: Albumin BCP Product Usage: ALBP is an in vitro test Recalled by Roche...

The Issue: The reagent lot is exhibiting calibration failures, QC imprecision, and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMarch 15, 2019· Estee Lauder Inc

Recalled Item: Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15 Recalled...

The Issue: Defective container: Ineffective seal between the cap and jar of the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Cleocin Phosphate Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Clindamycin Injection Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Clindamycin Injection Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Clindamycin Injection Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Cleocin Phosphate Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Cleocin Phosphate (clindamycin injection) Recalled by Pfizer Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 15, 2019· Response Biomedical Corp.

Recalled Item: Randox Laboratories Ltd. Catalogue Number CQ5052 Recalled by Response...

The Issue: The form received three complaints related to the user obtaining a result...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Panda Infant Radiant Warmer Infant radiant warmers provide infrared heat...

The Issue: The bedside panels and latch areas on the Giraffe Bedded Warmer and Panda...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat...

The Issue: The bedside panels and latch areas on the Giraffe Bedded Warmer and Panda...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Innova IGS 6 Recalled by GE Healthcare, LLC Due to There is a potential for...

The Issue: There is a potential for loss of the x-ray imaging function when the user...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Innova IGS 630 Recalled by GE Healthcare, LLC Due to There is a potential...

The Issue: There is a potential for loss of the x-ray imaging function when the user...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Innova IGS 630 Recalled by GE Healthcare, LLC Due to There is a potential...

The Issue: There is a potential for loss of the x-ray imaging function when the user...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMarch 14, 2019· Ata International Inc

Recalled Item: Blue Fusion Capsules Recalled by Ata International Inc Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Guided Start Drills/Counterbore NobRpl NP - Product Usage: The Guided...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Drill Tapered NP 3.5x11.5 mm Single-Pat - Product Usage: The Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Drill Tapered RP 4.3x11.5 mm Single-Pat - Product Usage: The Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing